Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
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id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
25421	MLL2	rs1190664201	SNP	missense variant	H/D	1497	1	0	942	probably damaging	0.941	27001	likely benign	27
25422	MLL2	rs1398611998	SNP	missense variant	T/I	1496	1	0	964	probably damaging	0.963	26001	likely benign	26
25423	MLL2	rs1348238080	SNP	missense variant	T/S	1496	91	0.09	788	possibly damaging	0.787	23001	likely benign	23
25424	MLL2	rs1472638183	SNP	missense variant	Y/C	1495	11	0.01	987	probably damaging	0.986	28001	likely benign	28
25425	MLL2	rs1005446890	SNP	missense variant	H/R	1488	591	0.59	133	benign	0.132	18001	likely benign	18
25426	MLL2	rs1339434307	SNP	missense variant	S/F	1484	1	0	897	possibly damaging	0.896	26001	likely benign	26
25427	MLL2	rs762536289	SNP	missense variant	A/V	1482	21	0.02	816	possibly damaging	0.815	27001	likely benign	27
25428	MLL2	rs565864326	SNP	missense variant	A/S	1482	251	0.25	160	benign	0.159	19001	likely benign	19
25429	MLL2	rs1242260574	SNP	missense variant	M/K	1478	21	0.02	389	benign	0.388	23001	likely benign	23
25430	MLL2	rs761478793	SNP	missense variant	M/V	1478	981	0.98	4	benign	0.003	15001	likely benign	15

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